Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c12 |
T |
A |
13: 4,320,212 (GRCm39) |
M293L |
possibly damaging |
Het |
Ankrd11 |
T |
C |
8: 123,621,683 (GRCm39) |
D723G |
probably benign |
Het |
Ankrd26 |
T |
C |
6: 118,500,442 (GRCm39) |
R1010G |
possibly damaging |
Het |
Apob |
G |
A |
12: 8,058,847 (GRCm39) |
R2410H |
probably benign |
Het |
Auh |
T |
C |
13: 52,992,165 (GRCm39) |
D275G |
probably damaging |
Het |
Card10 |
G |
T |
15: 78,686,822 (GRCm39) |
D47E |
possibly damaging |
Het |
Ccdc141 |
C |
T |
2: 76,859,579 (GRCm39) |
|
probably null |
Het |
Cfap206 |
T |
C |
4: 34,714,448 (GRCm39) |
Y416C |
possibly damaging |
Het |
Chuk |
A |
T |
19: 44,075,354 (GRCm39) |
Y500* |
probably null |
Het |
Cop1 |
T |
A |
1: 159,136,524 (GRCm39) |
D536E |
probably damaging |
Het |
Crh |
G |
C |
3: 19,748,304 (GRCm39) |
P113A |
possibly damaging |
Het |
Ddx54 |
T |
G |
5: 120,759,892 (GRCm39) |
|
probably null |
Het |
Efcab7 |
T |
C |
4: 99,769,793 (GRCm39) |
S127P |
probably damaging |
Het |
Efhc1 |
A |
G |
1: 21,030,442 (GRCm39) |
Y125C |
probably damaging |
Het |
Fga |
T |
A |
3: 82,938,848 (GRCm39) |
C408S |
probably damaging |
Het |
Flot2 |
T |
C |
11: 77,940,318 (GRCm39) |
S22P |
probably benign |
Het |
Fndc1 |
T |
A |
17: 7,991,672 (GRCm39) |
T675S |
unknown |
Het |
Foxc1 |
A |
G |
13: 31,992,836 (GRCm39) |
D549G |
unknown |
Het |
Gldc |
T |
C |
19: 30,111,162 (GRCm39) |
N538S |
possibly damaging |
Het |
Grk4 |
T |
G |
5: 34,888,894 (GRCm39) |
V346G |
probably damaging |
Het |
Gucy2c |
T |
C |
6: 136,747,127 (GRCm39) |
R111G |
probably benign |
Het |
Heatr6 |
C |
T |
11: 83,659,966 (GRCm39) |
H504Y |
probably damaging |
Het |
Lrp5 |
A |
T |
19: 3,670,013 (GRCm39) |
|
probably null |
Het |
Msrb1 |
T |
C |
17: 24,955,685 (GRCm39) |
S2P |
possibly damaging |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Myo3a |
A |
G |
2: 22,464,313 (GRCm39) |
I185V |
probably benign |
Het |
Myo5c |
T |
C |
9: 75,176,878 (GRCm39) |
S608P |
probably benign |
Het |
Nek6 |
A |
G |
2: 38,459,678 (GRCm39) |
I174V |
probably benign |
Het |
Nmt2 |
T |
C |
2: 3,315,766 (GRCm39) |
V252A |
probably damaging |
Het |
Nudt9 |
G |
T |
5: 104,207,545 (GRCm39) |
R179M |
probably damaging |
Het |
Nwd1 |
T |
C |
8: 73,383,690 (GRCm39) |
V29A |
possibly damaging |
Het |
Olah |
T |
C |
2: 3,343,964 (GRCm39) |
D216G |
possibly damaging |
Het |
Or13c7b |
T |
C |
4: 43,821,346 (GRCm39) |
N5S |
probably benign |
Het |
Or52n2 |
T |
C |
7: 104,542,719 (GRCm39) |
I39V |
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,795,461 (GRCm39) |
V2318A |
probably benign |
Het |
Pknox1 |
T |
A |
17: 31,807,534 (GRCm39) |
M51K |
probably damaging |
Het |
Ppp1r12a |
C |
T |
10: 108,098,242 (GRCm39) |
R321* |
probably null |
Het |
Pxdn |
A |
G |
12: 30,064,582 (GRCm39) |
|
probably null |
Het |
Rab44 |
A |
T |
17: 29,358,201 (GRCm39) |
I130F |
probably benign |
Het |
Rnf130 |
T |
C |
11: 49,962,091 (GRCm39) |
I179T |
probably damaging |
Het |
Slc22a28 |
A |
T |
19: 8,041,856 (GRCm39) |
C450* |
probably null |
Het |
Slco1c1 |
A |
T |
6: 141,485,778 (GRCm39) |
Y136F |
probably damaging |
Het |
Synj2 |
C |
T |
17: 6,067,844 (GRCm39) |
Q106* |
probably null |
Het |
Uckl1 |
T |
C |
2: 181,216,286 (GRCm39) |
N138S |
probably damaging |
Het |
Usp19 |
G |
T |
9: 108,376,018 (GRCm39) |
E203* |
probably null |
Het |
Vdr |
A |
G |
15: 97,755,386 (GRCm39) |
I379T |
probably damaging |
Het |
Zfp503 |
C |
A |
14: 22,036,101 (GRCm39) |
G272C |
probably damaging |
Het |
Zfyve9 |
T |
C |
4: 108,501,558 (GRCm39) |
N1218S |
possibly damaging |
Het |
Zzz3 |
T |
A |
3: 152,133,690 (GRCm39) |
D249E |
probably benign |
Het |
|
Other mutations in Parp12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02199:Parp12
|
APN |
6 |
39,073,524 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02937:Parp12
|
APN |
6 |
39,079,515 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03032:Parp12
|
APN |
6 |
39,064,520 (GRCm39) |
splice site |
probably null |
|
IGL03149:Parp12
|
APN |
6 |
39,091,165 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03365:Parp12
|
APN |
6 |
39,079,581 (GRCm39) |
missense |
probably damaging |
1.00 |
I1329:Parp12
|
UTSW |
6 |
39,064,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R1016:Parp12
|
UTSW |
6 |
39,088,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Parp12
|
UTSW |
6 |
39,079,495 (GRCm39) |
missense |
probably benign |
0.00 |
R1640:Parp12
|
UTSW |
6 |
39,088,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Parp12
|
UTSW |
6 |
39,073,574 (GRCm39) |
missense |
probably benign |
0.38 |
R4794:Parp12
|
UTSW |
6 |
39,094,744 (GRCm39) |
missense |
probably benign |
0.02 |
R5324:Parp12
|
UTSW |
6 |
39,079,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R5411:Parp12
|
UTSW |
6 |
39,067,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Parp12
|
UTSW |
6 |
39,088,670 (GRCm39) |
missense |
probably benign |
0.02 |
R6864:Parp12
|
UTSW |
6 |
39,088,670 (GRCm39) |
missense |
probably benign |
0.02 |
R7124:Parp12
|
UTSW |
6 |
39,088,670 (GRCm39) |
missense |
probably benign |
0.02 |
R7126:Parp12
|
UTSW |
6 |
39,088,670 (GRCm39) |
missense |
probably benign |
0.02 |
R7935:Parp12
|
UTSW |
6 |
39,079,612 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8050:Parp12
|
UTSW |
6 |
39,066,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8403:Parp12
|
UTSW |
6 |
39,068,279 (GRCm39) |
missense |
probably benign |
0.06 |
R8686:Parp12
|
UTSW |
6 |
39,094,856 (GRCm39) |
missense |
probably benign |
0.00 |
R8792:Parp12
|
UTSW |
6 |
39,065,984 (GRCm39) |
missense |
probably benign |
0.00 |
R8813:Parp12
|
UTSW |
6 |
39,073,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R9797:Parp12
|
UTSW |
6 |
39,067,185 (GRCm39) |
missense |
probably damaging |
0.99 |
|